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Levonorgestrel and Ethinyl Estradiol Tablet Manufacturing

Active

Federal

Response Deadline10/20/2026, 05:00:00 PM UTC

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

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This subcontract involves the manufacture of finished pharmaceutical tablets containing Levonorgestrel and Ethinyl Estradiol for the Department of Defense Medical Supply Chain. The contractor is responsible for producing medication compacts consisting of six cycles with 28 tablets per cycle, totaling 168 tablets per finished package using sequenced dosage. Production requires the use of pharmaceutical-grade tablet presses and USP-grade active pharmaceutical ingredients. To qualify, the manufacturer must be FDA registered and maintain strict compliance with USP standards, the Buy American Act, and the Berry Amendment. The project is categorized under NAICS code 325412, with the place of performance located at Fort Stewart. Interested parties must adhere to the response deadline of October 20, 2026.

General Info

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN PHARM FSA

NAICS

325412 - Pharmaceutical Preparation Manufacturing

Place of Performance

FORT STEWART, GA, 31314-5185, USA

Set-Aside

NONE

Documents

This scope was carved out of SPE2DP-27-T-0114.

The full solicitation package (1 document), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

LEVONORGESTREL AND

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Timeline

PostedOct 14

subcontract

Response DeadlineOct 20

Submission deadline

Response Deadline

10/20/2026, 05:00:00 PM UTCin 5 days

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Organization & Contact Information

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AgencyDepartment Of Defense → MEDICAL SUPPLY CHAIN PHARM FSA

ContactsNo contacts available

OfficeN/A

Organization / AgencyDepartment Of Defense → MEDICAL SUPPLY CHAIN PHARM FSA

Office AddressN/A

ContactsNo contact information available

Full Description

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Manufactures finished pharmaceutical tablets consisting of Levonorgestrel and Ethinyl Estradiol, USP for prime contractors on DLA Medical Supply Chain projects. Produces medication compacts of six cycles with 28 tablets per cycle using sequenced dosage. Requires pharmaceutical-grade tablet presses and USP-grade APIs. Must be FDA registered and compliant with USP standards, Buy American Act, and Berry Amendment. Delivers finished packages of 168 tablets.

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